Latest Cardiovascular Jobs

Senior Director Global Clinical Program Lead Cardiovascular & Renal

This role involves leading the clinical development of a medicine for cardiovascular and renal conditions, managing a cross-functional team, and ensuring compliance with regulatory standards. Responsibilities include strategic planning, clinical oversight, and authoring key documents for regulatory submissions and publications.

CSL Switzerland

On-site Permanent

Senior Director Global Clinical Program Lead Cardiovascular & Renal

This role involves leading the clinical development and strategic oversight of a medicine for cardiovascular and renal conditions. Responsibilities include managing the Clinical Development Team, ensuring high clinical and scientific standards, and authoring key study documents and regulatory submissions.

CSL

On-site Permanent

Head of Medical & Scientific Affairs - Cardiovascular, Renal & Metabolic

Leads national medical strategy for cardiovascular, renal, and metabolic therapies, shaping policy, driving NHS collaborations, and accelerating patient access to innovative treatments. Champions real-world evidence, scientific launch readiness, and cross-functional medical execution across the UK healthcare system.

AstraZeneca London, United Kingdom

Hybrid Permanent

Director, Clinical Intelligence & Evidence – Cardiovascular, Renal and Metabolism

Role: Director, Clinical Intelligence & Evidence – Cardiovascular, Renal and MetabolismLocation: Cambridge UKSalary: Competitive + Excellent BenefitsAt AstraZeneca make a meaningful impact that brings real benefits to society. By applying your knowledge of data, you will help to redefine our...

AstraZeneca Cambridge, United Kingdom

Global Labelling Associate Director, Content (Cardiovascular, Renal & Metabolism)

This role involves developing and maintaining global labelling strategies and documents for cardiovascular, renal, and metabolic products. You will lead cross-functional discussions, present labelling proposals, and ensure compliance with regulatory requirements across global markets.

Novartis London, United Kingdom

Hybrid Permanent

Global Labelling Associate Director, Content (Cardiovascular, Renal & Metabolism)

This role involves developing and maintaining global labelling strategies and core documents for cardiovascular, renal, and metabolic products. You will lead cross-functional discussions, present labelling proposals, and ensure compliance with regulatory requirements across global markets.

Novartis

Hybrid Permanent

Global Development Lead, Early Clinical Development, Internal Medicine

The Global Development Lead will drive clinical research for cardiometabolic diseases, creating and executing early clinical development strategies. They will work closely with cross-functional teams to translate pre-clinical observations into clinical experiments, ensuring medical and scientific excellence, and managing the delivery of clinical trial data and regulatory documents.

Pfizer Cambridge, United Kingdom

On-site Permanent

Global Development Lead, Early Clinical Development, Internal Medicine

The Global Development Lead will drive clinical research for cardiometabolic diseases, creating early clinical development strategies and leading the translation of pre-clinical observations into Phase 1/2 studies. They will work closely with cross-functional teams to ensure medical and scientific excellence, manage clinical trial execution, and engage with regulatory authorities and external collaborators.

Pfizer Sandwich, United Kingdom

On-site Permanent

Global Studies Asset Manager (GSAM)

The Global Asset Study Manager (GASM) at Roche/Genentech is responsible for the efficient execution of global clinical trials, ensuring consistency and compliance with IHC-GCP and Roche processes. Key responsibilities include coordinating study management, developing essential documents, driving innovation, and maintaining inspection readiness.

Roche Welwyn Hatfield, United Kingdom

On-site Permanent

Associate Director, Biostatistics 2

The role involves leading the statistical aspects of clinical development programs, including study design, data analysis, and regulatory submissions. Responsibilities include collaborating with cross-functional teams, managing CROs, and representing Biostatistics in regulatory interactions.

Appcast Enterprise Maidenhead, SL6 1QB, United Kingdom

On-site Permanent